A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5775n54



Internal ID20139199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75721290..75736441hg38UCSC Ensembl
chr17:73717370..73732522hg19UCSC Ensembl
chr17:71228965..71244117hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3815152
hg1915153
hg1815153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576034, nsv576035
Samples
Known GenesITGB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5775n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer